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Completed Phase 2 Interventional

Docetaxel, Gemcitabine, and Filgrastim (G-CSF) or Pegfilgrastim in Treating Patients With Advanced, Persistent, or Recurrent Uterine Leiomyosarcoma

ClinicalTrials.gov ID: NCT00101127

Public ClinicalTrials.gov record NCT00101127. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 10:52 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase II Evaluation of Docetaxel (NSC #628503) and Gemcitabine (NSC #613327) Plus G-CSF in the Treatment of Recurrent or Advanced Leiomyosarcoma of the Uterus

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

RATIONALE: Drugs used in chemotherapy, such as docetaxel and gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Colony-stimulating factors, such as G-CSF and pegfilgrastim, may increase the number of immune cells found in bone marrow or peripheral blood and may help the immune system recover from the side effects of chemotherapy. Giving docetaxel and gemcitabine together with G-CSF or pegfilgrastim may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving docetaxel and gemcitabine together with G-CSF or pegfilgrastim works in treating patients with advanced, persistent, or recurrent uterine leiomyosarcoma.

Study identification

NCT ID
NCT00101127
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Gynecologic Oncology Group
Network
Enrollment
Not listed

Conditions and interventions

Conditions

Interventions

Biological · Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 2003 (Type not available)
Primary completion
Jul 2006 (Actual)
Completion
Not listed
Last update posted
Feb 14, 2014

Started 2003

United States locations

U.S. sites
60
U.S. states
25
U.S. cities
50
Facility City State ZIP Site status
Kaiser Permanente Medical Center - Los Angeles Los Angeles California 90027 —
Jonsson Comprehensive Cancer Center at UCLA Los Angeles California 90095-1781 —
Helen and Harry Gray Cancer Center at Hartford Hospital Hartford Connecticut 06102-5037 —
New Britain General Hospital New Britain Connecticut 06050 —
CCOP - Christiana Care Health Services Newark Delaware 19713 —
MBCCOP-Medical College of Georgia Cancer Center Augusta Georgia 30912 —
Medical Center of Central Georgia Macon Georgia 31208 —
Curtis & Elizabeth Anderson Cancer Institute at Memorial Health University Medical Center Savannah Georgia 31403-3089 —
Rush-Copley Cancer Care Center Aurora Illinois 60507 —
Rush University Medical Center Chicago Illinois 60612 —
University of Chicago Cancer Research Center Chicago Illinois 60637-1470 —
Hinsdale Hematology Oncology Associates Hinsdale Illinois 60521 —
Joliet Oncology-Hematology Associates, Limited - West Joliet Illinois 60435 —
Carle Cancer Center at Carle Foundation Hospital Urbana Illinois 61801 —
CCOP - Carle Cancer Center Urbana Illinois 61801 —
Saint Anthony Memorial Health Centers Michigan City Indiana 46360 —
Holden Comprehensive Cancer Center at University of Iowa Iowa City Iowa 52242 —
Woman's Hospital Baton Rouge Louisiana 70815 —
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Baltimore Maryland 21231-2410 —
University of Mississippi Medical Center Jackson Mississippi 39216-4505 —
Ellis Fischel Cancer Center at University of Missouri - Columbia Columbia Missouri 65203 —
CCOP - Kansas City Kansas City Missouri 64131 —
CCOP - Cancer Research for the Ozarks Springfield Missouri 65802 —
St. John's Regional Health Center Springfield Missouri 65804 —
Hulston Cancer Center at Cox Medical Center South Springfield Missouri 65807 —
Siteman Cancer Center at Barnes-Jewish Hospital St Louis Missouri 63110 —
Methodist Cancer Center at Methodist Hospital - Omaha Omaha Nebraska 68114 —
Fox Chase Virtua Health Cancer Program - Marlton Marlton New Jersey 08053 —
UMDNJ University Hospital Newark New Jersey 07103 —
Cancer Institute of New Jersey at Cooper - Voorhees Voorhees Township New Jersey 08043 —
Fox Chase Virtua Health Cancer Program at Virtua West Jersey Voorhees Township New Jersey 08043 —
University of New Mexico Cancer Research and Treatment Center Albuquerque New Mexico 87131-5636 —
New York Oncology Hematology, PC at Albany Regional Cancer Care Albany New York 12208 —
SUNY Downstate Medical Center Brooklyn New York 11203 —
Stony Brook University Cancer Center Stony Brook New York 11794-8174 —
Hope A Women's Cancer Center Asheville North Carolina 28801 —
Lineberger Comprehensive Cancer Center at University of North Carolina - Chapel Hill Chapel Hill North Carolina 27599-7295 —
Duke Comprehensive Cancer Center Durham North Carolina 27710 —
Forsyth Regional Cancer Center at Forsyth Medical Center Winston-Salem North Carolina 27103 —
Wake Forest University Comprehensive Cancer Center Winston-Salem North Carolina 27157-1096 —
Charles M. Barrett Cancer Center at University Hospital Cincinnati Ohio 45267 —
Case Comprehensive Cancer Center Cleveland Ohio 44106 —
Cleveland Clinic Cancer Center at Fairview Hospital Cleveland Ohio 44111 —
Cleveland Clinic Taussig Cancer Center Cleveland Ohio 44195 —
Riverside Methodist Hospital Cancer Care Columbus Ohio 43214-3998 —
David L. Rike Cancer Center at Miami Valley Hospital Dayton Ohio 45409 —
Lake/University Ireland Cancer Center Mentor Ohio 44060 —
Oklahoma University Medical Center Oklahoma City Oklahoma 73104 —
Cancer Care Associates - Midtown Tulsa Tulsa Oklahoma 74104 —
Rosenfeld Cancer Center at Abington Memorial Hospital Abington Pennsylvania 19001 —
Penn State Cancer Institute at Milton S. Hershey Medical Center Hershey Pennsylvania 17033-0850 —
Drexel University College of Medicine - Center City Hahnemann Campus Philadelphia Pennsylvania 19102 —
Fox Chase Cancer Center Philadelphia Pennsylvania 19111-2497 —
Women and Infants Hospital of Rhode Island Providence Rhode Island 02905 —
Hollings Cancer Center at Medical University of South Carolina Charleston South Carolina 29425 —
Rapid City Regional Hospital Rapid City South Dakota 57701 —
Avera Cancer Institute Sioux Falls South Dakota 57105 —
Baptist Centers for Cancer Care Memphis Tennessee 38120 —
University of Virginia Cancer Center Charlottesville Virginia 22908 —
Gundersen Lutheran Cancer Center at Gundersen Lutheran Medical Center La Crosse Wisconsin 54601 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00101127, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 14, 2014 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00101127 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →